Activatable Fluorescent Probe for Studying Drug-Induced Senescence In Vitro and In Vivo.
Zihong LiPing HuangGuoliang WuWeiying LinPublished in: Analytical chemistry (2024)
Aging represents a significant risk factor for compromised tissue function and the development of chronic diseases in the human body. This process is intricately linked to oxidative stress, with HClO serving as a vital reactive oxygen species (ROS) within biological systems due to its strong oxidative properties. Hence, conducting a thorough examination of HClO in the context of aging is crucial for advancing the field of aging biology. In this work, we successfully developed a fluorescent probe, OPD , tailored specifically for detecting HClO in senescent cells and in vivo. Impressively, OPD exhibited a robust reaction with HClO, showcasing outstanding selectivity, sensitivity, and photostability. Notably, OPD effectively identified HClO in senescent cells for the first time, confirming that DOX- and ROS-induced senescent cells exhibited higher HClO levels compared to uninduced normal cells. Additionally, in vivo imaging of zebrafish demonstrated that d-galactose- and ROS-stimulated senescent zebrafish displayed elevated HClO levels compared to normal zebrafish. Furthermore, when applied to mouse tissues and organs, OPD revealed increased fluorescence in the organs of senescent mice compared to their nonsenescent counterparts. Our findings also illustrated the probe's potential for detecting changes in HClO content pre- and post-aging in living mice. Overall, this probe holds immense promise as a valuable tool for in vivo detection of HClO and for studying aging biology in live organisms.
Keyphrases
- induced apoptosis
- fluorescent probe
- living cells
- cell cycle arrest
- drug induced
- reactive oxygen species
- oxidative stress
- cell death
- liver injury
- endothelial cells
- endoplasmic reticulum stress
- risk assessment
- gene expression
- metabolic syndrome
- single molecule
- high fat diet induced
- smoking cessation
- skeletal muscle
- multidrug resistant
- single cell
- photodynamic therapy
- gram negative